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   1 geting the vasculature, GSCs, and GECs, using drugs already approved by the FDA, can reduce both tumor size and invasiven
     2  cyclic lipopeptide, is the only membrane-active antibiotic approved by the U.S. Food and Drug Administration so far.    
     3                        A number of injectable hydrogels are approved by FDA as surgery sealants, tissue adhesives, and ar
     4 golimod) is recognized as an immunosuppressant and has been approved by the Food and Drug Administration to treat refract
  
     6 selective androgen receptor modulators, which have not been approved by the US Food and Drug Administration (FDA), to enh
  
     8   A companion diagnostic is a test for a specific biomarker-approved by the United States Food and Drug Administration-qu
     9 tions and indications for active pharmaceutical ingredients approved by FDA and other regulatory agencies.               
    10 e comparative therapeutic value of all new cancer medicines approved by the US Food and Drug Administration (FDA) and the
    11 fibrillator (ICD) that was "non-MRI-conditional" (i.e., not approved by the Food and Drug Administration for MRI scanning
    12 tively from February 2012 through July 2015 under protocols approved by the local animal studies committee and institutio
    13 rapy with an HSV vector expressing GM-CSF has been recently approved by the Food and Drug Administration for the treatmen
    14 quency of postmarket safety events among novel therapeutics approved by the US Food and Drug Administration (FDA), and to
    15 ospective interpretation of prospectively acquired data was approved by the local ethics committee.                      
    16                    Left atrial appendage closure (LAAC) was approved by the U.S. Food and Drug Administration (FDA) as a 
    17               Materials and Methods The animal protocol was approved by the institutional animal care and use committee a
    18 cts provided written informed consent, and the protocol was approved by the university institutional review board.       
    19 rgeted oligonucleotide-based drug (nusinersen/Spinraza) was approved by US Food and Drug Administration (FDA) in late 201
    20                         Materials and Methods The study was approved by a research ethics committee, and participants gav
    21                         Materials and Methods The study was approved by institutional animal and human studies committees
  
    23            Materials and Methods This prospective study was approved by the ethics review board, and informed consent was
    24                         Materials and Methods The study was approved by the GE Global Research Center Institutional Anima
    25            Materials and Methods This prospective study was approved by the Institutional Animal Care and Use Committee. 
    26          Materials and Methods This retrospective study was approved by the institutional board review; written informed 
    27 als and Methods This single-center, retrospective study was approved by the institutional review board and compliant with
    28                        Materials and Methods This study was approved by the institutional review board and compliant with
    29                        Materials and Methods This study was approved by the institutional review board, and all participa
    30                        Materials and Methods This study was approved by the institutional review board, and written infor
  
  
  
  
    35 ls and Methods This HIPAA-compliant retrospective study was approved by the institutional review board; the requirement t
    36 terials and Methods This prospective case-control study was approved by the local ethics committee and the research depar
    37                         Materials and Methods The study was approved by the local Ethics Committee, and all patients or t
  
    39            Materials and Methods This prospective study was approved by the local ethics committees, and written informed
    40           Materials and Methods This case-control study was approved by the local research ethics committee.             
  
  
    43 ts from a prospective cohort study were included, which was approved by the local ethics board and written informed conse
    44                  Materials and Methods All experiments were approved by the institutional animal care and use committee. 
    45 ug/ml and disk diffusion (30/20-mug disk) test methods were approved by the CLSI Subcommittee on Antimicrobial Susceptibi
  
  
    48                        Materials and Methods Protocols were approved by the office of biologic safety and institutional a
    49 1358 individuals had died and had brain autopsies that were approved by board-certified neuropathologists.               
  
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